A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005962



Internal ID7071056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86406101..86409538hg38UCSC Ensembl
Outerchr9:89021016..89024453hg19UCSC Ensembl
Outerchr9:88210836..88214273hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg384112
hg194112
hg184112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565456
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005962
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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